Zhou Xing, Shi Min, Cao Jun, Yuan Tianwen, Yu Guanzhen, Chen Ying, Fang Wenzheng, Li Hongwei
Department of Interventional Oncology, Dahua Hospital, Shanghai, China.
Department of Pathology, Sichuan Cancer Center, School of Medicine, Sichuan Cancer Hospital & Institute, University of Electronic Science and Technology of China, Chengdu, China.
Front Genet. 2021 Jun 11;12:695036. doi: 10.3389/fgene.2021.695036. eCollection 2021.
Hepatocarcinogenesis is a highly complicated process that is promoted by a series of oncogenes. Our study aims to identify novel oncogenes promoting hepatocellular carcinoma (HCC) by bioinformatic analysis and experimental validation. Here, we reported that S100 calcium binding protein A10 (S100A10) was screened out as a potential novel oncogene in HCC by integrated analysis of OEP000321 dataset and the Cancer Genome Atlas (TCGA)-Liver-Cancer data. Furthermore, S100A10 was highly expressed in HCC samples and observably associated with patients' overall survival (OS). Overexpression of S100A10 in Hep3B and Huh-7 increased the cell proliferation, whereas downregulation of S100A10 in SK-Hep-1 and HepG2 cells reduced the cell viability to almost stop growing. tumor growth assays showed that S100A10-overexpressing Hep3B cells had a larger tumor size than control. Moreover, S100A10 overexpression promoted Hep3B cells migration and invasion, and S100A10 knockdown inhibited SK-Hep-1 cells migration and invasion, . In conclusion, it is demonstrated that S100A10 is a novel oncogene in HCC, indicating a possible novel therapeutic strategy of HCC.
肝癌发生是一个由一系列癌基因推动的高度复杂过程。我们的研究旨在通过生物信息学分析和实验验证来鉴定促进肝细胞癌(HCC)的新型癌基因。在此,我们报告通过对OEP000321数据集和癌症基因组图谱(TCGA)-肝癌数据的综合分析,筛选出S100钙结合蛋白A10(S100A10)作为HCC中一种潜在的新型癌基因。此外,S100A10在HCC样本中高表达,且与患者的总生存期(OS)显著相关。在Hep3B和Huh-7细胞中过表达S100A10可增加细胞增殖,而在SK-Hep-1和HepG2细胞中下调S100A10则使细胞活力降低至几乎停止生长。肿瘤生长实验表明,过表达S100A10的Hep3B细胞的肿瘤体积大于对照组。此外,S100A10过表达促进Hep3B细胞迁移和侵袭,而敲低S100A10则抑制SK-Hep-1细胞迁移和侵袭。总之,已证明S100A10是HCC中的一种新型癌基因,这为HCC指明了一种可能的新型治疗策略。